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Dedicated to successful NIV
Hospital respiratory care
V60 ventilator
Specifi cations
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Specifi cations
3. Settings
Settings Range
C-Flex OFF, 1 – 3
CPAP 4 – 25cmH2O
EPAP 4 – 25cmH2O
IPAP 4 – 40cmH2O
I-time (inspiratory time) 0.30 – 3.00sec
Max P (AVAPS maximum IPAP) 6 – 40cmH2O
Min P (AVAPS minimum IPAP) 5 – 30cmH2O
O2 (oxygen percent) 21 – 100%
Ramp time OFF, 5 – 45min
Rate (respiratory rate) 4 – 60bpm
Rise (rise time) 1 – 5
Triggering and cycling Auto-adaptive (Auto-Trak)
AVAPS target tidal volume 200 – 2,000ml btps
Max E 0 – 100cmH2O/I
Max R 0 – 50cmH2O/l/s
PPV% 0 – 100%
Max P (PPV maximum pressure limit) 5 – 40cmH2O
Max V (PPV maximum volume limit) 200 – 3,500ml
The Philips Respironics V60 ventilator combines Respironics’ ventilation expertise with Philips focus on simplifying advanced health care. The result is exceptional noninvasive ventilation with an invasive ventilation fallback and an interactive display that helps simplify patient management.
* May not be available in all markets
1. Patient types
Adult
Pediatric (≥20kg)
2. Modes
Standard
CPAP (continuous positive airway pressure)
S/T (spontaneous with timed backup)
PCV (pressure control ventilation)
AVAPS (average volume assured pressure support)
Optional
PPV (proportional pressure ventilation)*
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4. Modes with settings
CPAP S/T PCV AVAPS PPV
Rate
I-time
CPAP
EPAP
IPAP
Rise
Min P
Max P
Max V
Max E
Max R
PPV%
O2
VT (tidal volume)
C-Flex
Ramp time
5. Monitored parameters
Patient data window
Breath phase/trigger indicator Spont, timed, exhale
PIP 0 – 50cmH2O
Patient/total leak 0 – 200l/min btps
Patient trigger 0 – 100%
Respiratory rate 0 – 90bpm
Ti/Ttot 0 – 91%
Minute volume 0 – 99.0l/min btps
Tidal volume 0 – 3,500ml btps
Waveform window
Pressure waveform 0 – 50cmH2O
Flow waveform -240 – 240l/min btps
Volume waveform 0 – 3,500ml btps
6. Alarms
Alarm Adjustable range
Hi Rate (high respiratory rate alarm) 5 – 90bpm
Lo Rate (low respiratory rate alarm) 1 – 89bpm
Hi VT (high tidal volume alarm) 200 – 3,500ml
Lo VT (low tidal volume alarm) Off, 5 – 1,500ml
HIP (high inspiratory pressure alarm) 5 – 50cmH2O
LIP (low inspiratory pressure alarm) OFF, 1 – 40cmH2O
Lo VE (low minute ventilation alarm) OFF, 0.1 – 99l/min
LIP T (low inspiratory pressure delay time)
5 – 60sec
7. Other settings
Alarm volume 1 – 10 (relative scale)
Brightness 1 – 5 (relative scale)
Exhalation port selection • DEP (disposable exhalation port)
• Whisper Swivel• PEV (plateau exhalation
valve)• Other• None (no inline circuit
exhalation port)
Interface selection ET/Trach, 1, 2, 3, Other
Screen lock Off, On
Auto-Trak Plus Optional*
Trigger* Normal, 1 – 7
E-cycle* -2, -1, Normal, 1 – 6
8. Environmental
Temperature
Operating conditions +5 – +40ºC
Storage conditions -20 – +50ºC
Relative humidity
Operating conditions 15 – 95% (non-condensing)
Storage conditions 10 – 95% (non-condensing)
Barometric pressure
Operation and storage 79.9 – 101.1kPa(600 – 765mmHg)
Altitude
Operation and storage 600 to 765 mmHg (approximately -61 to 1951m (-200 to 6400 ft) relative to sea level)
* May not be available in all markets
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© 2016 Koninklijke Philips N.V. All rights reserved.Specifications are subject to change without notice.
Bernoulli is a registered trademark of Cardiopulmonary Corp.DataCaptor is a trademark of CapsuleTech.CareAware, and iBusare trademarks of Cerner Corp.
www.philips.com
4522 991 22601 * OCT 2016
9. Communication
Philips IntelliBridge EC10
Philips IntelliBridge EC40/80
Philips VueLink Open Interface
Respi-Link remote diagnostic system
Bernoulli® management system
Capsule DataCaptorTM device interface driver
GE Healthcare (Centricty Critical Care)
Cerner CareAware® iBus™
Other monitoring and patient information systems
RS232 digital and analog
10. Electrical
External
AC voltage 100 – 240 VAC
AC frequency 50/60Hz
AC power 300 VA
Battery (optional)
Nominal voltage 14.4V
Capacity 11.0Ah
Battery chemistry Lithium-ion
Operating time 6 hours in normal conditions
12. Regulatory compliance
2nd edition standards
EN 60601-1-2 Electromagnetic Compatibility Requirements and Tests
EN 55011 Radiated and Conducted RF Disturbance Characteristics--Limits and Methods of Measurement (Level A)
EN 55014-1 Electromagnetic Compatibility Requirements. Part 1: Emissions
EN 61000-3-2 Limits for Harmonic Current Emissions
EN 61000-3-3 Limitation of Voltage Changes, Fluctuations, and Flicker Emissions
EN 61000-4-2 Electrostatic Discharge Immunity Test (8/15KV)
11. Physical
Weight 11.7kg (25.7lb) with optional battery10.6kg (23.3lb) without optional battery
Dimensions 33.7cm (13.3in) height39.4cm (15.5in) width42.9cm (16.5in) depth
Please visit www.philips.com/V60
EN 61000-4-3 Radiated Electromagnetic Field Immunity Test (10V/M)
EN 61000-4-4 Electrical Fast Transient/Burst Immunity Test
EN 61000-4-5 Surge Immunity Test
EN 61000-4-6 Immunity to Conducted RF Disturbances (10V)
EN 61000-4-8 Power Frequency Magnetic Field Immunity Test
EN 61000-4-11 Voltage Dips, Short Interruptions, and Voltage Variations Immunity Tests
MIL-STD 461E RE101
Electromagnetic Field Generation (Army Level)
ANSI/AAMI ES 60601-1
Medical electrical equipment - Part 1: General requirements for basic safety and essential performance
WEEE recycling directive
Compliant with the WEEE recycling directive
3rd edition standards
IEC 60601-1; Ed. 3.1
Medical electrical equipment – Part 1: General requirements form basic safety and essential performance
IEC 60601-1-2; Ed. 3.0
Medical electrical equipment - Part 1-2: General requirements for basic safety and essential performance - Collateral Standard: Electromagnetic disturbances
IEC 60601-1-6; 2013
Medical electrical equipment – Part 1-6: General requirements for safety
IEC 60601-1-8; Ed. 2.1
Medical electrical equipment – Part 1-8: General requirements for safety
IEC 62366; 2007 + A1: 2004
Medical devices - Application of usability engineering to medical devices
ISO 14971; 2007
Medical devices – Application of risk management to medical devices
EN ISO 14971; 2012
Medical devices – Application of risk management to medical devices
ISO 80601-2-12; 2011
Medical electrical equipment – Particular requirements for basic safety and essential performance of critical care ventilators
ISO 60529; Ed. 2.1
Degrees of protection provided by enclosures (IPX1 @ 0° tilt)
IEC 62304; Ed. 1.0
Medical device software - Software life cycle processes
ANSI/AAMI ES 60601-1
Medical electrical equipment - Part 1: General requirements for basic safety and essential performance
WEEE recycling directive
Compliant with the WEEE recycling directive
The print quality of this copy is not an accurate representation of the original.